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Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium
Vascular networks within a living organism are complex, multi-dimensional, and challenging to image capture. Radio-angiographic studies in live animals require a high level of infrastructure and technical investment in order to administer costly perfusion mediums whose signals metabolize and degrade...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078938/ https://www.ncbi.nlm.nih.gov/pubmed/21533123 http://dx.doi.org/10.1371/journal.pone.0019099 |
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author | Vasquez, Sergio X. Gao, Feng Su, Feng Grijalva, Victor Pope, John Martin, Bill Stinstra, Jeroen Masner, Matthew Shah, Neha Weinstein, David M. Farias-Eisner, Robin Reddy, Srinivasa T. |
author_facet | Vasquez, Sergio X. Gao, Feng Su, Feng Grijalva, Victor Pope, John Martin, Bill Stinstra, Jeroen Masner, Matthew Shah, Neha Weinstein, David M. Farias-Eisner, Robin Reddy, Srinivasa T. |
author_sort | Vasquez, Sergio X. |
collection | PubMed |
description | Vascular networks within a living organism are complex, multi-dimensional, and challenging to image capture. Radio-angiographic studies in live animals require a high level of infrastructure and technical investment in order to administer costly perfusion mediums whose signals metabolize and degrade relatively rapidly, diminishing within a few hours or days. Additionally, live animal specimens must not be subject to long duration scans, which can cause high levels of radiation exposure to the specimen, limiting the quality of images that can be captured. Lastly, despite technological advances in live-animal specimen imaging, it is quite difficult to minimize or prevent movement of a live animal, which can cause motion artifacts in the final data output. It is demonstrated here that through the use of postmortem perfusion protocols of radiopaque silicone polymer mediums and ex-vivo organ harvest, it is possible to acquire a high level of vascular signal in preclinical specimens through the use of micro-computed tomographic (microCT) imaging. Additionally, utilizing high-order rendering algorithms, it is possible to further derive vessel morphometrics for qualitative and quantitative analysis. |
format | Text |
id | pubmed-3078938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30789382011-04-29 Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium Vasquez, Sergio X. Gao, Feng Su, Feng Grijalva, Victor Pope, John Martin, Bill Stinstra, Jeroen Masner, Matthew Shah, Neha Weinstein, David M. Farias-Eisner, Robin Reddy, Srinivasa T. PLoS One Research Article Vascular networks within a living organism are complex, multi-dimensional, and challenging to image capture. Radio-angiographic studies in live animals require a high level of infrastructure and technical investment in order to administer costly perfusion mediums whose signals metabolize and degrade relatively rapidly, diminishing within a few hours or days. Additionally, live animal specimens must not be subject to long duration scans, which can cause high levels of radiation exposure to the specimen, limiting the quality of images that can be captured. Lastly, despite technological advances in live-animal specimen imaging, it is quite difficult to minimize or prevent movement of a live animal, which can cause motion artifacts in the final data output. It is demonstrated here that through the use of postmortem perfusion protocols of radiopaque silicone polymer mediums and ex-vivo organ harvest, it is possible to acquire a high level of vascular signal in preclinical specimens through the use of micro-computed tomographic (microCT) imaging. Additionally, utilizing high-order rendering algorithms, it is possible to further derive vessel morphometrics for qualitative and quantitative analysis. Public Library of Science 2011-04-18 /pmc/articles/PMC3078938/ /pubmed/21533123 http://dx.doi.org/10.1371/journal.pone.0019099 Text en Vasquez et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Vasquez, Sergio X. Gao, Feng Su, Feng Grijalva, Victor Pope, John Martin, Bill Stinstra, Jeroen Masner, Matthew Shah, Neha Weinstein, David M. Farias-Eisner, Robin Reddy, Srinivasa T. Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium |
title | Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium |
title_full | Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium |
title_fullStr | Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium |
title_full_unstemmed | Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium |
title_short | Optimization of MicroCT Imaging and Blood Vessel Diameter Quantitation of Preclinical Specimen Vasculature with Radiopaque Polymer Injection Medium |
title_sort | optimization of microct imaging and blood vessel diameter quantitation of preclinical specimen vasculature with radiopaque polymer injection medium |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078938/ https://www.ncbi.nlm.nih.gov/pubmed/21533123 http://dx.doi.org/10.1371/journal.pone.0019099 |
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